A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656535



Internal ID9922640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116579230..116579525hg38UCSC Ensembl
chr8:117591469..117591764hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6398082, essv5952149, essv6170209, essv6576952, essv6454677, essv5769373, essv6101897, essv5415111, essv5796143, essv5908792, essv6079189, essv6535469, essv5721579, essv6021819, essv5525935, essv5749416, essv6544534, essv6377557, essv6549874, essv5554709, essv5794977, essv5707276, essv6525823, essv6204025, essv5768674, essv6105710, essv5919446, essv6140245, essv6366288, essv5511948, essv6263751, essv6457762, essv5460811, essv6173832, essv5966903, essv5947972, essv6198523, essv6265366, essv6063871, essv6135742, essv5473751, essv6314592, essv5559260, essv6178467, essv5429960, essv5812081, essv6597171, essv6173157, essv6441593, essv6531452, essv6449250, essv6531651, essv5518997, essv6377003, essv6493142, essv6091146, essv5485431, essv6189621, essv6518786, essv5566296, essv6073234, essv5983516, essv6249802, essv6293018, essv5578368, essv5776853, essv6524591, essv5709721, essv6105184, essv6485115, essv6337186, essv6064560, essv5891987, essv6383321, essv5417136, essv6111229, essv6120161, essv6553417, essv6507503, essv5704604, essv6150941, essv5467092, essv6543730, essv5918212, essv6269643
SamplesNA19394, NA18502, NA19700, NA19397, NA18924, NA18947, NA18508, NA18980, NA19704, NA18507, NA11920, NA18917, NA12045, NA19355, NA19393, NA19443, NA19190, NA19920, NA18510, NA19374, NA19373, NA19379, NA18550, NA18519, NA19315, NA18942, NA18916, NA19313, NA19384, NA20291, NA19130, NA19383, NA18874, NA12156, NA19372, NA19238, NA19172, NA19471, HG01440, NA19456, NA18867, NA19451, NA11993, NA12489, NA19707, NA19391, NA18516, NA19982, NA18910, NA18856, NA18912, NA12892, NA18853, NA19099, NA19452, NA19225, NA19318, NA19395, NA19625, NA19401, NA19390, NA11881, NA19108, NA19147, NA18517, NA19331, NA19380, NA19835, NA19334, NA19428, NA19324, NA18943, NA19248, NA19472, NA19093, NA18873, NA19116, NA19711, NA19129, HG01111, NA18968, NA19463, NA18511, NA18522, NA19346
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656535
Frequency
Sample Size1151
Observed Gain0
Observed Loss85
Observed Complex0
Frequencyn/a


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